Bringing the future into focus

Publications 2009

  1. Barkhuysen R, Nielsen CC, Klevering BJ, Van Damme PA. 2009. The transconjunctival approach with lateral canthal extension for three-wall orbital decompression in thyroid orbitopathy. J Craniomaxillofac Surg 37:127-131.
  2. Boon CJ, Klevering BJ, Cremers FP, Zonneveld-Vrieling MN, Theelen T, den Hollander AI, Hoyng CB. 2009a. Central areolar choroidal dystrophy. Ophthalmology 116:771-82, 782.
  3. Boon CJ, Klevering BJ, Leroy BP, Hoyng CB, Keunen JE, den Hollander AI. 2009b. The spectrum of ocular phenotypes caused by mutations in the BEST1 gene. Prog Retin Eye Res 28:187-205.
  4. Boon CJ, Theelen T, Hoefsloot EH, van Schooneveld MJ, Keunen JE, Cremers FP, Klevering BJ, Hoyng CB. 2009c. Clinical and molecular genetic analysis of best vitelliform macular dystrophy. Retina 29:835-847.
  5. Boon CJ, Theelen T, Hoyng CB. 2009d. Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity. Am J Ophthalmol 148:173-174.
  6. Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI. 2009e. The spectrum of phenotypes caused by variants in the CFH gene. Mol Immunol 46:1573-1594.
  7. Caramoy A, Lappas A, Fauser S, Kirchhof B. 2009a. [Central scotoma and blurred vision in a patient with Crohn's disease.]. Ophthalmologe.
  8. Caramoy A, Liakopoulos S, Menrath E, Kirchhof B. 2009b. Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: Long term functional and anatomical outcome. Br J Ophthalmol.
  9. den Hollander AI, McGee TL, Ziviello C, Banfi S, Dryja TP, Gonzalez-Fernandez F, Ghosh D, Berson EL. 2009. A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci 50:1864-1872.
  10. Joussen AM, Lux A, Kirchhof B. 2009a. Shifting of the proliferative vitreoretinopathy milieu after tamponade with heavy silicone oil in eyes prone to proliferative vitreoretinopathy and bleeding. Br J Ophthalmol 93:128-129.
  11. Joussen AM, Wong D, Walter P, Kirchhof B, Dreyhaupt J, Bauer C, Munzinger J, Unnebrink K, Freiberger A, Seibert-Grafe M, Victor N. 2009b. Surgical management of subfoveal choroidal neovascular membranes in age-related macular degeneration by macular relocation: experiences of an early-stopped randomised clinical trial (MARAN Study). Eye.
  12. Keane PA, Bhatti RA, Brubaker JW, Liakopoulos S, Sadda SR, Walsh AC. 2009a. Comparison of clinically relevant findings from high-speed fourier-domain and conventional time-domain optical coherence tomography. Am J Ophthalmol 148:242-248.
  13. Keane PA, Chang KT, Liakopoulos S, Jivrajka RV, Walsh AC, Sadda SR. 2009b. Effect of ranibizumab retreatment frequency on neurosensory retinal volume in neovascular amd. Retina 29:592-600.
  14. Keane PA, Liakopoulos S, Jivrajka RV, Chang KT, Alasil T, Walsh AC, Sadda SR. 2009c. Evaluation of optical coherence tomography retinal thickness parameters for use in clinical trials for neovascular age-related macular degeneration. Invest Ophthalmol Vis Sci 50:3378-3385.
  15. Keane PA, Liakopoulos S, Walsh AC, Sadda SR. 2009d. Limits of the retinal-mapping program in age-related macular degeneration. Br J Ophthalmol 93:274-275.
  16. Keane PA, Mand PS, Liakopoulos S, Walsh AC, Sadda SR. 2009e. Accuracy of Retinal Thickness Measurements obtained with Cirrus Optical Coherence Tomography. Br J Ophthalmol.
  17. Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, den Hollander AI, Zonneveld MN, Othman MI, Waseem N, Chakarova CF, Maubaret C, az-Font A, Macdonald I, Muzny DM, Wheeler DA, Morgan M, Lewis LR, Logan CV, Tan PL, Beer MA, Inglehearn CF, Lewis RA, Jacobson SG, Bergmann C, Beales PL, ttie-Bitach T, Johnson CA, Otto EA, Bhattacharya SS, Hildebrandt F, Gibbs RA, Koenekoop RK, Swaroop A, Katsanis N. 2009. A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nat Genet.
  18. Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI. 2009. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder. Invest Ophthalmol Vis Sci 50:2344-2350.
  19. Theelen T, Berendschot TT, Hoyng CB, Boon CJ, Klevering BJ. 2009. Near-infrared reflectance imaging of neovascular age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol.
  20. Thiadens AA, den Hollander AI, Roosing S, Nabuurs SB, Zekveld-Vroon RC, Collin RW, De BE, Koenekoop RK, van Schooneveld MJ, Strom TM, van Lith-Verhoeven JJ, Lotery AJ, van Moll-Ramirez N, Leroy BP, van den Born LI, Hoyng CB, Cremers FP, Klaver CC. 2009a. Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders. Am J Hum Genet 85:240-247.
  21. Thiadens AA, Slingerland NW, Roosing S, van Schooneveld MJ, van Lith-Verhoeven JJ, van Moll-Ramirez N, van den Born LI, Hoyng CB, Cremers FP, Klaver CC. 2009b. Genetic Etiology and Clinical Consequences of Complete and Incomplete Achromatopsia. Ophthalmology.
  22. Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RW, Hoyng CB, Lopez I, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK, Chen R. 2009. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. Am J Hum Genet 84:380-387.